ACS Publications. Most Trusted. Most Cited. Most Read
Probing the Dynamics of Protein–Protein Interactions at Neuronal Contacts by Optical Imaging

OR SEARCH CITATIONS

My Activity
Publications

Figure 1Loading Img
Download Hi-Res ImageDownload to MS-PowerPointCite This:Chem. Rev. 2008, 108, 5, 1565-1587
    Review

    Probing the Dynamics of Protein–Protein Interactions at Neuronal Contacts by Optical Imaging
    Click to copy article linkArticle link copied!

    View Author Information
    CNRS UMR 5091, Institut Magendie, Université Bordeaux 2, 33077 Bordeaux, France, Leibniz Institüt für Neurobiologie, Magdeburg, Germany, PICIN, Institut Magendie, Université Bordeaux 2, 33077 Bordeaux, France, and Centre de Physique Moléculaire Optique et Hertzienne, CNRS-Université Bordeaux 1, 33405 Talence, France
    * Corresponding authors. E-mail: [email protected]; [email protected]
    †CNRS UMR 5091, Institut Magendie, Université Bordeaux 2.
    ‡Leibniz Institüt für Neurobiologie.
    §PICIN, Institut Magendie, Université Bordeaux 2.
    ⊥Centre de Physique Moléculaire Optique et Hertzienne, CNRS-Université Bordeaux 1.
    Other Access Options

    Chemical Reviews

    Cite this: Chem. Rev. 2008, 108, 5, 1565–1587
    Click to copy citationCitation copied!
    https://doi.org/10.1021/cr078204m
    Published May 1, 2008
    Copyright © 2008 American Chemical Society
    Request reuse permissions
    Copyright © 2008 American Chemical Society

    Subjects

    what are subjects

    Note: In lieu of an abstract, this is the article's first page.

    Free first page

    Read this article

    To access this article, please review the available access options below.

    Get instant access

    Purchase Access

    Read this article for 48 hours. Check out below using your ACS ID or as a guest.

    Recommended

    Access through Your Institution

    You may have access to this article through your institution.

    Your institution does not have access to this content. Add or change your institution or let them know you’d like them to include access.

    Cited By

    Click to copy section linkSection link copied!
    Citation Statements
    Explore this article's citation statements on scite.ai
    powered by  Scite

    This article is cited by 53 publications.

    1. Arnaud Tron, Isabelle Pianet, Alberto Martinez-Cuezva, James H. R. Tucker, Luca Pisciottani, Mateo Alajarin, Jose Berna, and Nathan D. McClenaghan . Remote Photoregulated Ring Gliding in a [2]Rotaxane via a Molecular Effector. Organic Letters 2017, 19 (1) , 154-157. https://doi.org/10.1021/acs.orglett.6b03457
    2. Hong-Min Meng, Zhen Jin, Yifan Lv, Chan Yang, Xiao-Bing Zhang, Weihong Tan, and Ru-Qin Yu . Activatable Two-Photon Fluorescence Nanoprobe for Bioimaging of Glutathione in Living Cells and Tissues. Analytical Chemistry 2014, 86 (24) , 12321-12326. https://doi.org/10.1021/ac503617n
    3. Zhichao Dai, Lu Tian, Bo Song, Zhiqiang Ye, Xiangli Liu, and Jingli Yuan . Ratiometric Time-Gated Luminescence Probe for Hydrogen Sulfide Based on Lanthanide Complexes. Analytical Chemistry 2014, 86 (23) , 11883-11889. https://doi.org/10.1021/ac503611f
    4. Hua Zhang, Jiangli Fan, Kui Wang, Jing Li, Caixia Wang, Yamin Nie, Tao Jiang, Huiying Mu, Xiaojun Peng, and Kai Jiang . Highly Sensitive Naphthalene-Based Two-Photon Fluorescent Probe for in Situ Real-Time Bioimaging of Ultratrace Cyclooxygenase-2 in Living Biosystems. Analytical Chemistry 2014, 86 (18) , 9131-9138. https://doi.org/10.1021/ac501944y
    5. Jun Yao, Mei Yang, and Yixiang Duan . Chemistry, Biology, and Medicine of Fluorescent Nanomaterials and Related Systems: New Insights into Biosensing, Bioimaging, Genomics, Diagnostics, and Therapy. Chemical Reviews 2014, 114 (12) , 6130-6178. https://doi.org/10.1021/cr200359p
    6. Yuanwei Zhang, Xiling Yue, Bosung Kim, Sheng Yao, Mykhailo V. Bondar, and Kevin D. Belfield . Bovine Serum Albumin Nanoparticles with Fluorogenic Near-IR-Emitting Squaraine Dyes. ACS Applied Materials & Interfaces 2013, 5 (17) , 8710-8717. https://doi.org/10.1021/am402361w
    7. Guo-Jiang Mao, Tian-Tian Wei, Xu-Xiang Wang, Shuang-yan Huan, Dan-Qing Lu, Jing Zhang, Xiao-Bing Zhang, Weihong Tan, Guo-Li Shen, and Ru-Qin Yu . High-Sensitivity Naphthalene-Based Two-Photon Fluorescent Probe Suitable for Direct Bioimaging of H2S in Living Cells. Analytical Chemistry 2013, 85 (16) , 7875-7881. https://doi.org/10.1021/ac401518e
    8. Masayori Suwa, Yusuke Nakano, Satoshi Tsukahara, and Hitoshi Watarai . Faraday Rotation Dispersion Microscopy Imaging of Diamagnetic and Chiral Liquids with Pulsed Magnetic Field. Analytical Chemistry 2013, 85 (10) , 5176-5183. https://doi.org/10.1021/ac400541k
    9. Jian Zhang, Yi Fu, Cecil V. Conroy, Zhenghua Tang, Ge Li, Richard Y. Zhao, and Gangli Wang . Fluorescence Intensity and Lifetime Cell Imaging with Luminescent Gold Nanoclusters. The Journal of Physical Chemistry C 2012, 116 (50) , 26561-26569. https://doi.org/10.1021/jp306036y
    10. Yi-Jun Gong, Xiao-Bing Zhang, Cui-Cui Zhang, Ai-Li Luo, Ting Fu, Weihong Tan, Guo-Li Shen, and Ru-Qin Yu . Through Bond Energy Transfer: A Convenient and Universal Strategy toward Efficient Ratiometric Fluorescent Probe for Bioimaging Applications. Analytical Chemistry 2012, 84 (24) , 10777-10784. https://doi.org/10.1021/ac302762d
    11. Jian Zhang, Yi Fu, and Joseph R. Lakowicz . Fluorescent Metal Nanoshells: Lifetime-Tunable Molecular Probes in Fluorescent Cell Imaging. The Journal of Physical Chemistry C 2011, 115 (15) , 7255-7260. https://doi.org/10.1021/jp111475y
    12. Essa Mayyas, Margarida Bernardo, Lindsay Runyan, Anjum Sohail, Venkatesh Subba-Rao, Mircea Pantea, Rafael Fridman, and Peter M. Hoffmann . Dissociation Kinetics of an Enzyme−Inhibitor System Using Single-Molecule Force Measurements. Biomacromolecules 2010, 11 (12) , 3352-3358. https://doi.org/10.1021/bm100844x
    13. Yuu Someya and Hiroharu Yui . Fluorescence Lifetime Probe for Solvent Microviscosity Utilizing Anilinonaphthalene Sulfonate. Analytical Chemistry 2010, 82 (13) , 5470-5476. https://doi.org/10.1021/ac100116j
    14. Mikhail Y. Berezin and Samuel Achilefu. Fluorescence Lifetime Measurements and Biological Imaging. Chemical Reviews 2010, 110 (5) , 2641-2684. https://doi.org/10.1021/cr900343z
    15. Zhi-Xiang Han, Xiao-Bing Zhang, Zhuo Li, Yi-Jun Gong, Xiang-Yang Wu, Zhen Jin, Chun-Mei He, Li-Xin Jian, Jing Zhang, Guo-Li Shen and Ru-Qin Yu. Efficient Fluorescence Resonance Energy Transfer-Based Ratiometric Fluorescent Cellular Imaging Probe for Zn2+ Using a Rhodamine Spirolactam as a Trigger. Analytical Chemistry 2010, 82 (8) , 3108-3113. https://doi.org/10.1021/ac100376a
    16. Chun-Yan Li, Xiao-Bing Zhang, Li Qiao, Yan Zhao, Chun-Mei He, Shuang-Yan Huan, Li-Min Lu, Li-Xin Jian, Guo-Li Shen and Ru-Qin Yu. Naphthalimide−Porphyrin Hybrid Based Ratiometric Bioimaging Probe for Hg2+: Well-Resolved Emission Spectra and Unique Specificity. Analytical Chemistry 2009, 81 (24) , 9993-10001. https://doi.org/10.1021/ac9018445
    17. Yan Zhao, Xiao-Bing Zhang, Zhi-Xiang Han, Li Qiao, Chun-Yan Li, Li-Xin Jian, Guo-Li Shen and Ru-Qin Yu. Highly Sensitive and Selective Colorimetric and Off−On Fluorescent Chemosensor for Cu2+ in Aqueous Solution and Living Cells. Analytical Chemistry 2009, 81 (16) , 7022-7030. https://doi.org/10.1021/ac901127n
    18. Jian Zhang, Yi Fu, Dong Liang, Richard Y. Zhao and Joseph R. Lakowicz . Fluorescent Avidin-Bound Silver Particle: A Strategy for Single Target Molecule Detection on a Cell Membrane. Analytical Chemistry 2009, 81 (3) , 883-889. https://doi.org/10.1021/ac801932m
    19. Dongni Han, Bertrand Goudeau, Dragan Manojlovic, Dechen Jiang, Danjun Fang, Neso Sojic. Electrochemiluminescence Loss in Photobleaching. Angewandte Chemie 2021, 133 (14) , 7764-7768. https://doi.org/10.1002/ange.202015030
    20. Dongni Han, Bertrand Goudeau, Dragan Manojlovic, Dechen Jiang, Danjun Fang, Neso Sojic. Electrochemiluminescence Loss in Photobleaching. Angewandte Chemie International Edition 2021, 60 (14) , 7686-7690. https://doi.org/10.1002/anie.202015030
    21. Laurent Groc, Daniel Choquet. Linking glutamate receptor movements and synapse function. Science 2020, 368 (6496) https://doi.org/10.1126/science.aay4631
    22. Xiaodong Wang, Lu An, Qiwei Tian, Kuili Cui. Recent progress in H 2 S activated diagnosis and treatment agents. RSC Advances 2019, 9 (58) , 33578-33588. https://doi.org/10.1039/C9RA06698E
    23. . Intracellular oxygen mapping using a myoglobin-mCherry probe with fluorescence lifetime imaging. Journal of Biomedical Optics 2018, 1. https://doi.org/10.1117/1.JBO.23.10.107001
    24. Mingxiang Gao, Jinyu Li, Cunbin Nie, Beibei Song, Lin Yan, Hai Qian. Design, synthesis and biological evaluation of novel hydrogen sulfide releasing capsaicin derivatives. Bioorganic & Medicinal Chemistry 2018, 26 (9) , 2632-2639. https://doi.org/10.1016/j.bmc.2018.04.031
    25. Yiren Wang, Huan Wang, Mei Yang, Jingli Yuan, Jing Wu. A visible-light-excited europium(III) complex-based luminescent probe for visualizing copper ions and hydrogen sulfide in living cells. Optical Materials 2018, 75 , 243-251. https://doi.org/10.1016/j.optmat.2017.10.030
    26. Hong-Wen Liu, Yongchao Liu, Peng Wang, Xiao-Bing Zhang. Molecular engineering of two-photon fluorescent probes for bioimaging applications. Methods and Applications in Fluorescence 2017, 5 (1) , 012003. https://doi.org/10.1088/2050-6120/aa61b0
    27. Anuji K Vasu, Mahalingavelar Paramasivam, Sriram Kanvah. Carbohydrate Tethered Cyanostilbene Fluorogen: Unique Emission and Preferential Protein Binding. ChemistrySelect 2017, 2 (1) , 405-414. https://doi.org/10.1002/slct.201601709
    28. Qianqian Qiu, Xin Deng, Lei Jiao, Tianxiao Zhao, Fanfei Meng, Wenlong Huang, Hai Qian. A High‐Sensitivity Coumarin‐Based Fluorescent Probe for Monitoring Hydrogen Sulfide in Living Cells. Chemical Biology & Drug Design 2015, 86 (2) , 173-179. https://doi.org/10.1111/cbdd.12483
    29. Dmitry A. Nedosekin, Stephen Foster, Zeid A. Nima, Alexandru S. Biris, Ekaterina I. Galanzha, Vladimir P. Zharov. Photothermal confocal multicolor microscopy of nanoparticles and nanodrugs in live cells. Drug Metabolism Reviews 2015, 47 (3) , 346-355. https://doi.org/10.3109/03602532.2015.1058818
    30. Bin Xiong, Lan Peng, Xuan Cao, Yan He, Edward S. Yeung. Optical analysis of biological hydrogen sulphide: an overview of recent advancements. The Analyst 2015, 140 (6) , 1763-1771. https://doi.org/10.1039/C4AN02204A
    31. Xue-Lin Shi, Guo-Jiang Mao, Xiao-Bing Zhang, Hong-Wen Liu, Yi-Jun Gong, Yong-Xiang Wu, Li-Yi Zhou, Jing Zhang, Weihong Tan. Rhodamine-based fluorescent probe for direct bio-imaging of lysosomal pH changes. Talanta 2014, 130 , 356-362. https://doi.org/10.1016/j.talanta.2014.07.030
    32. Dmitry A. Nedosekin, Ekaterina I. Galanzha, Enkeleda Dervishi, Alexandru S. Biris, Vladimir P. Zharov. Super‐Resolution Nonlinear Photothermal Microscopy. Small 2014, 10 (1) , 135-142. https://doi.org/10.1002/smll.201300024
    33. Zhi-Xiang Han, Bo-Song Zhu, Tong-Liang Wu, Qing-Qing Yang, Yong-Lai Xue, Zhen Zhang, Xiang-Yang Wu. A fluorescent probe for Hg2+ sensing in solutions and living cells with a wide working pH range. Chinese Chemical Letters 2014, 25 (1) , 73-76. https://doi.org/10.1016/j.cclet.2013.10.027
    34. Junpei Yuasa, Ryusuke Mukai, Yasuchika Hasegawa, Tsuyoshi Kawai. Ratiometric luminescence thermometry based on crystal-field alternation at the extremely narrow 5D0 → 7F2 transition band of europium(iii). Chemical Communications 2014, 50 (59) , 7937. https://doi.org/10.1039/c4cc00704b
    35. Tianyue Zhang, Guowei Lu, Wenqiang Li, Jie Liu, Lei Hou, Pascal Perriat, Matteo Martini, Olivier Tillement, Qihuang Gong. Optimally Designed Nanoshell and Matryoshka-Nanoshell as a Plasmonic-Enhanced Fluorescence Probe. The Journal of Physical Chemistry C 2012, 116 (15) , 8804-8812. https://doi.org/10.1021/jp2125944
    36. Dmitry A. Nedosekin, Ekaterina I. Galanzha, Srinivas Ayyadevara, Robert J. Shmookler Reis, Vladimir P. Zharov. Photothermal Confocal Spectromicroscopy of Multiple Cellular Chromophores and Fluorophores. Biophysical Journal 2012, 102 (3) , 672-681. https://doi.org/10.1016/j.bpj.2011.12.035
    37. Satyabrata Si, Cecile Leduc, Marie‐Hélène Delville, Brahim Lounis. Short Gold Nanorod Growth Revisited: The Critical Role of the Bromide Counterion. ChemPhysChem 2012, 13 (1) , 193-202. https://doi.org/10.1002/cphc.201100710
    38. Paresh Chandra Ray, Anant Kumar Singh, Dulal Senapati, Sadia Afrin Khan, Wentong Lu, Lule Beqa, Zhen Fan, Samuel S. R. Dasary, Tahir Arbneshi. Nanomaterial-Based Long-Range Optical Ruler for Monitoring Biomolecular Activities. 2012, 159-183. https://doi.org/10.1007/978-1-4614-0884-0_6
    39. Martin Heine. Surface Traffic in Synaptic Membranes. 2012, 197-219. https://doi.org/10.1007/978-3-7091-0932-8_9
    40. Michael B. Steketee, Jeffrey L. Goldberg. Signaling Endosomes and Growth Cone Motility in Axon Regeneration. 2012, 35-73. https://doi.org/10.1016/B978-0-12-407178-0.00003-X
    41. Magali Mondin, Virginie Labrousse, Eric Hosy, Martin Heine, Béatrice Tessier, Florian Levet, Christel Poujol, Christophe Blanchet, Daniel Choquet, Olivier Thoumine. Neurexin-Neuroligin Adhesions Capture Surface-Diffusing AMPA Receptors through PSD-95 Scaffolds. The Journal of Neuroscience 2011, 31 (38) , 13500-13515. https://doi.org/10.1523/JNEUROSCI.6439-10.2011
    42. Chunwei Yu, Lingxin Chen, Jun Zhang, Jinhua Li, Ping Liu, Wenhai Wang, Bing Yan. “Off-On” based fluorescent chemosensor for Cu2+ in aqueous media and living cells. Talanta 2011, 85 (3) , 1627-1633. https://doi.org/10.1016/j.talanta.2011.06.057
    43. Bo Chen, Laura C. Estrada, Christian Hellriegel, Enrico Gratton. Nanometer-scale optical imaging of collagen fibers using gold nanoparticles. Biomedical Optics Express 2011, 2 (3) , 511. https://doi.org/10.1364/BOE.2.000511
    44. PARESH CHANDRA RAY, HONGTAO YU, PETER P. FU. Nanogold-Based Sensing of Environmental Toxins: Excitement and Challenges. Journal of Environmental Science and Health, Part C 2011, 29 (1) , 52-89. https://doi.org/10.1080/10590501.2011.551315
    45. Frédéric Boal, Michel Laguerre, Alexandra Milochau, Jochen Lang, Pier A. Scotti. A charged prominence in the linker domain of the cysteine‐string protein Cspα mediates its regulated interaction with the calcium sensor synaptotagmin 9 during exocytosis. The FASEB Journal 2011, 25 (1) , 132-143. https://doi.org/10.1096/fj.09-152033
    46. Yuu SOMEYA, Hiroharu YUI. Measurements of Microproperties of Water Utilizing Charge-Transfer Dye Anilinonaphthalene Sulfonate. BUNSEKI KAGAKU 2011, 60 (1) , 11-18. https://doi.org/10.2116/bunsekikagaku.60.11
    47. Osamu Hayashida, Chika Eguchi, Keiichiro Kimura, Yu Oyama, Tomomi Nakashima, Kosei Shioji. Guest Binding, Cellular Uptake, and Molecular Delivery of Water-soluble Cyclophanes Having a Pyrene Moiety. Chemistry Letters 2010, 39 (12) , 1321-1322. https://doi.org/10.1246/cl.2010.1321
    48. Wenhai Wang, Afu Fu, Jingbo Lan, Ge Gao, Jingsong You, Lijuan Chen. Rational Design of Fluorescent Bioimaging Probes by Controlling the Aggregation Behavior of Squaraines: A Special Effect of Ionic Liquid Pendants. Chemistry – A European Journal 2010, 16 (17) , 5129-5137. https://doi.org/10.1002/chem.200903492
    49. Damien Alcor, Géraldine Gouzer, Antoine Triller. Single‐particle tracking methods for the study of membrane receptors dynamics. European Journal of Neuroscience 2009, 30 (6) , 987-997. https://doi.org/10.1111/j.1460-9568.2009.06927.x
    50. PARESH CHANDRA RAY, HONGTAO YU, PETER P. FU. Toxicity and Environmental Risks of Nanomaterials: Challenges and Future Needs. Journal of Environmental Science and Health, Part C 2009, 27 (1) , 1-35. https://doi.org/10.1080/10590500802708267
    51. Nancy J. Woolf, Avner Priel, Jack A. Tuszynski. Nanocarriers and Intracellular Transport: Moving Along the Cytoskeletal Matrix. 2009, 129-176. https://doi.org/10.1007/978-3-642-03584-5_4
    52. Olivier Thoumine, et al. et al.. ChemInform Abstract: Probing the Dynamics of Protein—Protein Interactions at Neuronal Contacts by Optical Imaging. ChemInform 2008, 39 (37) https://doi.org/10.1002/chin.200837273
    53. Antoine Triller, Daniel Choquet. New Concepts in Synaptic Biology Derived from Single-Molecule Imaging. Neuron 2008, 59 (3) , 359-374. https://doi.org/10.1016/j.neuron.2008.06.022
    Download PDF
    Go to Chemical Reviews
    Get e-Alerts
    Get e-Alerts

    Chemical Reviews

    Cite this: Chem. Rev. 2008, 108, 5, 1565–1587
    Click to copy citationCitation copied!
    https://doi.org/10.1021/cr078204m
    Published May 1, 2008
    Copyright © 2008 American Chemical Society
    Request reuse permissions

    Article Views

    2423

    Altmetric

    -

    Citations

    53
    Learn about these metrics

    Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.

    Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.

    The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated.